ClinVar Miner

List of variants in gene PTEN reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP
NM_000314.4(PTEN):c.1104T>C (p.Asp368=) rs35979531
NM_000314.6(PTEN):c.*10T>A rs769236743
NM_000314.6(PTEN):c.1197A>G (p.Gln399=) rs374684043
NM_000314.6(PTEN):c.132C>T (p.Gly44=) rs150651961
NM_000314.6(PTEN):c.210-7_210-3del5 rs587780544
NM_000314.7(PTEN):c.-246C>T rs886047393
NM_000314.7(PTEN):c.235G>A (p.Ala79Thr) rs202004587

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.